New diabetes drug SHR-3167 takes on insulin in Head-to-Head trial
NCT ID NCT06688123
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new medicine called SHR-3167 against a standard insulin (insulin glargine) for people with type 2 diabetes. About 275 adults who are not on insulin yet, but take metformin (alone or with another diabetes drug), will receive either SHR-3167 or insulin glargine. The main goal is to see which treatment better lowers blood sugar levels (HbA1c) over 20 weeks, while also checking for side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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275 people
The number who actually took part.
- Started
-
Jan 2025
- Finished
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Apr 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Able and willing to provide a written informed consent. 2. Diagnosed with type 2 diabetes mellitus ≥ 6 months prior to the day of screening. 3. A stable dose of metformin alone or in combination with a stable dose of a SGLT2 inhibitor for 3 months prior to screening. 4. Body mass index (BMI): 18.5\~35.0 kg/m2. 5. HbA1c of 7.5%\~10.0% as assessed by the local laboratory. 6. Insulin naïve. 7. Female subjects and partners of male subjects who are of childbearing potential, have no fertility plan and agree to take highly effective contraceptive measures within 6 months after signing the informed consent form to the last dose, and have no plans to donate eggs/sperm; Female subjects of childbearing potential have a negative pregnancy test during the screening period and are not lactating. Exclusion Criteria: 1. Electrocardiogram (ECG) results show clinically significant abnormalities that may affect the safety of the subject. 2. Poor blood pressure control at screening. 3. Diagnosis or suspicion of type 1 diabetes mellitus, latent autoimmune diabetes mellitus in adult (LADA),other special types of diabetes or secondary diabetes mellitus. 4. ≥1 episode of severe hypoglycemia or asymptomatic hypoglycemia within 6 months prior to screening, or recurrent hypoglycemic events within 1 month prior to screening. 5. History of diabetic ketoacidosis or hyperosmolar hyperglycemic state due to hyperglycemia within 6 months prior to screening. 6. Presence of acute or chronic hepatitis, cirrhosis, or other serious liver disease other than non-alcoholic fatty liver disease. 7. Those who have a history of severe cardiovascular and cerebrovascular diseases within 6 months before screening. 8. Malignancy or history of malignancy within 5 years prior to screening. 9. Received any diabetes mellitus or weight-loss medication outside the inclusion criteria within 3 months prior to screening. 10. Participation in a clinical trial of any drug or medical device within 3 months prior to screening. 11. Any other condition judged by the investigator to be likely to affect the subject's safety or interfere with the evaluation of trial results.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Jiangsu Provincial People's Hospital
Nanjing, Jiangsu, 210029, China
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Shanghai Sixth People's Hospital
Shanghai, Shanghai Municipality, 200233, China
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